FDA UDI In Commercial Distribution 🇺🇸 United States

Polyurethane Dual Lumen Occlusion Catheter

DI: 00840663102259 · Model: 4F-2L-40 · Lemaitre Vascular, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Polyurethane Dual Lumen Occlusion Catheter
Primary DI
00840663102259
Version / Model
4F-2L-40
Catalog Number
4F-2L-40
Company Name
Lemaitre Vascular, Inc.
Labeler DUNS
184805166
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-06-30
Public Version
6
Public Version Date
2023-12-04
Public Version Status
Update
Public Device Record Key
4e07f6cc-2aa4-4f6b-8327-0eb8012e4d97

Device Description

Polyurethane Dual Lumen Occlusion Catheter, 4F, 40cm

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DQT Occluder, Catheter Tip

GMDN Terms

Code Name
32584 Intravascular occluding balloon catheter, image-guided

Identifiers

Type ID
Primary 00840663102259

Customer Contacts

Phone
781-221-2266

Premarket Submissions

Submission Number Supplement Number
K844918 000